Please choose an event type to view the corresponding MedsFacts report:

DIARRHOEA ( 8 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
THROAT IRRITATION ( 5 FDA reports)
SWELLING ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
MUSCLE STRAIN ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 5 FDA reports)
PAIN ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
CONSTIPATION ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
MALAISE ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VOMITING ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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